Filtering small nucleic acids using permeabilized cells

ABSTRACT

Filtering small nucleic acids using permeabilized cells and methods for using the filtering to detect genomic DNA accessibility are described.

CROSS-REFERENCE TO RELATED PATENT APPLICATIONS

The present patent application claims benefit of priority to U.S.Provisional Patent Application Nos. 61/514,711, filed Aug. 3, 2011 and61/570,581, filed Dec. 14, 2011, each of which are incorporated byreference.

BACKGROUND OF THE INVENTION

Chromatin is classified into two main groups, euchromatin, where the DNAis loosely packaged, accessible and generally, but not always,transcriptionally competent, and heterochromatin, where the DNA istightly packaged, inaccessible and generally, but not always,transcriptionally silent.

Epigenetics controls at least some of the transition between these twochromatin states. There are at least two main epigenetic events: DNAmethylation and histone modification. These events affect how the DNA ispackaged and whether the DNA is active or silent with respect totranscription.

BRIEF SUMMARY OF THE INVENTION

The present invention provides, e.g., methods of separating DNAaccessible to a DNA cleaving agent in a permeabilized cell from DNAinaccessible to the DNA cleaving agent. In some embodiments, the methodcomprises: permeabilizing a cell having genomic DNA, thereby generatinga permeabilized cell; introducing a DNA cleaving agent into thepermeabilized cell having genomic DNA under conditions such that the DNAcleaving agent cleaves the genomic DNA in the cell, thereby generatingcleaved DNA; and separating cleaved DNA that diffuses out of the intactpermeabilized cell from the cell.

In some embodiments, the method further comprises introducing a DNAmodifying agent into the permeabilized cell such that the DNA modifyingagent modifies the genomic DNA in the cell. In some embodiments, the DNAmodifying agent and the DNA cleaving agent are introduced simultaneouslyor the DNA modifying agent is introduced before the DNA cleaving agentis introduced. In some embodiments, the DNA cleaving agent is DNase I ormicrococcal nuclease. In some embodiments, the DNA modifying agent addsmodifications to at least some recognition sequences of the DNA cleavingagent, and the DNA cleaving agent does not cleave recognition sequenceswith the modification. In some embodiments, the DNA modifying agent addsmodifications to at least some recognition sequences of the DNA cleavingagent, and the DNA cleaving agent cleaves recognition sequences with themodification and does not cleave recognition sequences lacking themodification.

In some embodiments, the DNA modifying agent is a DNA methyltransferase.In some embodiments, the DNA modifying agent is introduced after the DNAcleaving agent is introduced.

In some embodiments, the permeabilizing and the introducing occursimultaneously.

In some embodiments, the method further comprises isolating the cleavedDNA.

In some embodiments, the method further comprises isolating DNAremaining in the intact cell following the separating.

In some embodiments, the cell is permeabilized with a permeabilizationagent. In some embodiments, the cell is permeabilized by electroporationor biolistics. In some embodiments, the permeabilization agent is alysolipid or a nonionic detergent.

In some embodiments, the DNA cleaving agent comprises a DNase. In someembodiments, the DNA cleaving agent is DNase I or micrococcal nuclease.

In some embodiments, the DNA cleaving agent comprises a restrictionenzyme. In some embodiments, the restriction enzyme is a methylationsensing restriction enzyme. In some embodiments, the restriction enzymeis a N⁶-methyl adenosine sensing restriction enzyme. In someembodiments, the restriction enzyme is a methyl cytosine sensingrestriction enzyme. In some embodiments, the restriction enzyme is a5-hydroxymethyl cytosine-sensing restriction enzyme. In someembodiments, the restriction enzyme cleaves a recognition sequencecomprising a 5′-hydroxymethylcytosine.

In some embodiments, the DNA cleaving agent comprises a DNA cleavingpolypeptide fused to a heterologous DNA-recognition polypeptide.

In some embodiments, the DNA cleaving agent comprises a DNA cleavingpolypeptide fused to a heterologous protein-recognition polypeptide.

In some embodiments, the isolating comprises affinity purifying the DNA.In some embodiments, the affinity purifying comprisesimmunoprecipitating. In some embodiments, the DNA is affinity purifiedby binding an affinity agent to a protein associated with the DNA,thereby purifying the protein and DNA associated with the protein. Insome embodiments, the affinity agent is an antibody. In someembodiments, the affinity agent is linked to a solid support. In someembodiments, the protein associated with the DNA is a histone, amodified histone (modified (e.g., methylated) or not), a transcriptionfactor, an RNA polymerase or a TATA box-binding protein (TBP).

In some embodiments, the isolated DNA is from about 50 bp to about 10kb.

In some embodiments, the method further comprises analyzing theseparated DNA. In some embodiments, the analyzing comprises nucleotidesequencing the separated DNA. In some embodiments, the nucleotidesequencing further detects DNA modifications. In some embodiments, theanalyzing comprises an amplification reaction. In some embodiments, theanalyzing comprises nucleic acid hybridization. In some embodiments, twoor more nucleic acids are associated with one or more proteins and theanalyzing comprises ligating the two or more nucleic acids.

In some embodiments, the isolated DNA is associated with one or moreprotein. In some embodiments, the method further comprises analyzing theone or more protein associated with the isolated DNA.

In some embodiments, the isolated DNA is associated with one or moreRNA. In some embodiments, the method further comprises analyzing the oneor more RNA associated with the isolated DNA.

In some embodiments, the separating comprises centrifuging and/orfiltering the permeabilized cell thereby separating a solutioncontaining the cleaved DNA from the cell. In some embodiments, a DNAmodification agent was introduced into the permeabilized cell and theanalyzing comprises determining the presence or absence of modificationsin the isolated DNA.

The present invention also provides for kits, e.g., comprising one ormore reagent as described herein for use with the methods describedherein. In some embodiments, the kit comprises a DNA modifying agentand/or a DNA cleaving agent; a cell permeabilization agent; and anaffinity agent that specifically binds to a DNA-binding protein.

In some embodiments, the DNA cleaving agent comprises a DNase or arestriction enzyme or a DNA cleaving polypeptide fused to a heterologousDNA-recognition polypeptide. In some embodiments, the DNA modifyingagent is a DNA methyltransferase. In some embodiments, thepermeabilization agent is a lysolipid or a nonionic detergent. In someembodiments, the affinity agent specifically binds to a histone, an RNApolymerase, a transcription factor, or a TATA box-binding protein (TBP).In some embodiments, the affinity agent is linked to a solid support. Insome embodiments, the solid support is a bead or particle. In someembodiments, the bead or particle is magnetic.

DEFINITIONS

“Permeabilizing,” a cell membrane, as used herein, refers to reducingthe integrity of a cell membrane, thereby allowing smaller genomic DNAfragments or protein-DNA/histone DNA complexes to diffuse from thecells, and optionally to allow for entry of a DNA cleaving and/ormodifying agent, or other enzyme proteins, antibodies or chimericproteins into the cell. A cell with a permeabilized cell membrane willgenerally retain the cell membrane such that the cell's structureremains substantially intact. A cell with a permeabilized membrane isnot a “lysed” cell, for example as occurs in standard DNA purificationtechniques. In contrast, “disrupting” a cell membrane, as used herein,refers to reducing the integrity of a cell membrane such that the cell'sstructure does not remain intact (e.g., such as during cell lysis).

A “DNA modifying agent,” as used herein, refers to a molecule thatalters DNA in a detectable manner. Exemplary modifications include DNAcleavage, DNA nicking, or introduction or removal of chemical moietiesfrom the DNA (generally wherein the introduction or removal does notdirectly result in cleavage of the DNA). DNA modifying agents include,but are not limited to, DNA methyltransferases.

A “DNA region,” as used herein, refers to a target sequence of interestwithin genomic DNA. The DNA region can be of any length that is ofinterest and that is accessible by the DNA modifying agent being used.In some embodiments, the DNA region can include a single base pair, butcan also be a short segment of sequence within genomic DNA (e.g., 2-100,2-500, 50-500 bp) or a larger segment (e.g., 100-10,000,100-1000, or1000-5000 bp. The amount of DNA in a DNA region is sometimes determinedby the amount of sequence to be amplified in a PCR reaction (i.e.,between two primers). For example, standard PCR reactions generally canamplify between about 35 to 5000 base pairs.

A different “extent” of modifications refers to a different number(actual or relative) of modified copies of one or more DNA regionsbetween samples or between two or more DNA regions in one or moresamples. For example, if 100 copies of two DNA regions (designated forconvenience as “region A” and “region B”) are each present inchromosomal DNA in a cell, an example of modification to a differentextent would be if 10 copies of region A were modified whereas 70 copiesof region B were modified.

The terms “oligonucleotide” or “polynucleotide” or “nucleic acid”interchangeably refer to a polymer of monomers that can be correspondedto a ribose nucleic acid (RNA) or deoxyribose nucleic acid (DNA)polymer, or analog thereof. This includes polymers of nucleotides suchas RNA and DNA, as well as modified forms thereof, peptide nucleic acids(PNAs), locked nucleic acids (LNA™), and the like. In certainapplications, the nucleic acid can be a polymer that includes multiplemonomer types, e.g., both RNA and DNA subunits.

A nucleic acid is typically single-stranded or double-stranded and willgenerally contain phosphodiester bonds, although in some cases, asoutlined herein, nucleic acid analogs are included that may havealternate backbones, including, for example and without limitation,phosphoramide (Beaucage et al. (1993) Tetrahedron 49(10):1925 and thereferences therein; Letsinger (1970) J. Org. Chem. 35:3800; Sprinzl etal. (1977) Eur. J. Biochem. 81:579; Letsinger et al. (1986) Nucl. AcidsRes. 14: 3487; Sawai et al. (1984) Chem. Lett. 805; Letsinger et al.(1988) J. Am. Chem. Soc. 110:4470; and Pauwels et al. (1986) ChemicaScripta 26:1419), phosphorothioate (Mag et al. (1991) Nucleic Acids Res.19:1437 and U.S. Pat. No. 5,644,048), phosphorodithioate (Briu et al.(1989) J. Am. Chem. Soc. 111:2321), O-methylphosphoroamidite linkages(Eckstein, Oligonucleotides and Analogues: A Practical Approach, OxfordUniversity Press (1992)), and peptide nucleic acid backbones andlinkages (Egholm (1992) J. Am. Chem. Soc. 114:1895; Meier et al. (1992)Chem. Int. Ed. Engl. 31:1008; Nielsen (1993) Nature 365:566; andCarlsson et al. (1996) Nature 380:207), which references are eachincorporated by reference. Other analog nucleic acids include those withpositively charged backbones (Denpcy et al. (1995) Proc. Natl. Acad.Sci. USA 92:6097); non-ionic backbones (U.S. Pat. Nos. 5,386,023,5,637,684, 5,602,240, 5,216,141 and 4,469,863; Angew (1991) Chem. Intl.Ed. English 30: 423; Letsinger et al. (1988) J. Am. Chem. Soc. 110:4470;Letsinger et al. (1994) Nucleoside & Nucleotide 13:1597; Chapters 2 and3, ASC Symposium Series 580, “Carbohydrate Modifications in AntisenseResearch”, Ed. Y. S. Sanghvi and P. Dan Cook; Mesmaeker et al. (1994)Bioorganic & Medicinal Chem. Lett. 4: 395; Jeffs et al. (1994) J.Biomolecular NMR 34:17; Tetrahedron Lett. 37:743 (1996)) and non-ribosebackbones, including those described in U.S. Pat. Nos. 5,235,033 and5,034,506, and Chapters 6 and 7, ASC Symposium Series 580, CarbohydrateModifications in Antisense Research, Ed. Y. S. Sanghvi and P. Dan Cook,which references are each incorporated by reference. Nucleic acidscontaining one or more carbocyclic sugars are also included within thedefinition of nucleic acids (Jenkins et al. (1995) Chem. Soc. Rev. pp169-176, which is incorporated by reference). Several nucleic acidanalogs are also described in, e.g., Rawls, C & E News Jun. 2, 1997 page35, which is incorporated by reference. These modifications of theribose-phosphate backbone may be done to facilitate the addition ofadditional moieties such as labeling moieties, or to alter the stabilityand half-life of such molecules in physiological environments.

In addition to naturally occurring heterocyclic bases that are typicallyfound in nucleic acids (e.g., adenine, guanine, thymine, cytosine, anduracil), nucleic acid analogs also include those having non-naturallyoccurring heterocyclic or other modified bases, many of which aredescribed, or otherwise referred to, herein. In particular, manynon-naturally occurring bases are described further in, e.g., Seela etal. (1991) Hely. Chim. Acta 74:1790, Grein et al. (1994) Bioorg. Med.Chem. Lett. 4:971-976, and Seela et al. (1999) Hely. Chim. Acta 82:1640,which are each incorporated by reference. To further illustrate, certainbases used in nucleotides that act as melting temperature (Tm) modifiersare optionally included. For example, some of these include7-deazapurines (e.g., 7-deazaguanine, 7-deazaadenine, etc.),pyrazolo[3,4-d]pyrimidines, propynyl-dN (e.g., propynyl-dU, propynyl-dC,etc.), and the like. See, e.g., U.S. Pat. No. 5,990,303, entitled“SYNTHESIS OF 7-DEAZA-2′-DEOXYGUANOSINE NUCLEOTIDES,” which issued Nov.23, 1999 to Seela, which is incorporated by reference. Otherrepresentative heterocyclic bases include, e.g., hypoxanthine, inosine,xanthine; 8-aza derivatives of 2-aminopurine, 2,6-diaminopurine,2-amino-6-chloropurine, hypoxanthine, inosine and xanthine;7-deaza-8-aza derivatives of adenine, guanine, 2-aminopurine,2,6-diaminopurine, 2-amino-6-chloropurine, hypoxanthine, inosine andxanthine; 6-azacytosine; 5-fluorocytosine; 5-chlorocytosine;5-iodocytosine; 5-bromocytosine; 5-methylcytosine; 5-propynylcytosine;5-bromovinyluracil; 5-fluorouracil; 5-chlorouracil; 5-iodouracil;5-bromouracil; 5-trifluoromethyluracil; 5-methoxymethyluracil;5-ethynyluracil; 5-propynyluracil, and the like.

“Accessibility” of a DNA region to a DNA modifying agent, as usedherein, refers to the ability of a particular DNA region in a chromosomeof a cell to be contacted and modified by a particular DNA modifyingagent. Without intending to limit the scope of the invention, it isbelieved that the particular chromatin structure comprising the DNAregion will affect the ability of a DNA modifying agent to modify theparticular DNA region. For example, the DNA region may be wrapped aroundhistone proteins and further may have additional nucleosomal structurethat prevents, or reduces access of, the DNA modifying agent to the DNAregion of interest.

The phrase “specifically (or selectively) binds” refers to a bindingreaction that is determinative of the presence of the target (e.g., atarget protein) in a heterogeneous population of proteins and otherbiologics. For example, under immunoassay conditions, antibodies orother protein recognition polypeptides bind to a particular protein atleast two times background and do not substantially bind in asignificant amount to other proteins present in the sample. Typically aspecific or selective reaction will be at least twice background signalor noise and more typically more than 10 to 100 times background.

“Antibody” refers to a polypeptide comprising a framework region from animmunoglobulin gene or fragments thereof that specifically binds andrecognizes an antigen. The recognized immunoglobulin genes include thekappa, lambda, alpha, gamma, delta, epsilon, and mu constant regiongenes, as well as the myriad immunoglobulin variable region genes. Lightchains are classified as either kappa or lambda. Heavy chains areclassified as gamma, mu, alpha, delta, or epsilon, which in turn definethe immunoglobulin classes, IgG, IgM, IgA, IgD and IgE, respectively.

Naturally occurring immunoglobulins have a common core structure inwhich two identical light chains (about 24 kD) and two identical heavychains (about 55 or 70 kD) form a tetramer. The amino-terminal portionof each chain is known as the variable (V) region and can bedistinguished from the more conserved constant (C) regions of theremainder of each chain. Within the variable region of the light chainis a C-terminal portion known as the J region. Within the variableregion of the heavy chain, there is a D region in addition to the Jregion. Most of the amino acid sequence variation in immunoglobulins isconfined to three separate locations in the V regions known ashypervariable regions or complementarity determining regions (CDRs)which are directly involved in antigen binding. Proceeding from theamino-terminus, these regions are designated CDR1, CDR2 and CDR3,respectively. The CDRs are held in place by more conserved frameworkregions (FRs). Proceeding from the amino-terminus, these regions aredesignated FR1, FR2, FR3, and FR4, respectively. The locations of CDRand FR regions and a numbering system have been defined by, e.g., Kabatet al. (Kabat et al., Sequences of Proteins of Immunological Interest,Fifth Edition, U.S. Department of Health and Human Services, U.S.Government Printing Office (1991)).

An exemplary immunoglobulin (antibody) structural unit comprises atetramer. Each tetramer is composed of two identical pairs ofpolypeptide chains, each pair having one “light” (about 25 kDa) and one“heavy” chain (about 50-70 kDa). The N-terminus of each chain defines avariable region of about 100 to 110 or more amino acids primarilyresponsible for antigen recognition. The terms variable light chain(V_(L)) and variable heavy chain (V_(H)) refer to these light and heavychains respectively.

Antibodies can exist, e.g., as intact immunoglobulins or as a number ofwell-characterized fragments produced by digestion with variouspeptidases. Thus, for example, pepsin digests an antibody below thedisulfide linkages in the hinge region to produce F(ab)′₂, a dimer ofFab which itself is a light chain joined to V_(H)-C_(H1) by a disulfidebond. The F(ab)′₂ may be reduced under mild conditions to break thedisulfide linkage in the hinge region, thereby converting the F(ab)′₂dimer into an Fab′ monomer. The Fab′ monomer is essentially Fab withpart of the hinge region (see FUNDAMENTAL IMMUNOLOGY (Paul ed., 3d ed.1993). While various antibody fragments are defined in terms of thedigestion of an intact antibody, one of skill will appreciate that suchfragments may be synthesized de novo either chemically or by usingrecombinant DNA methodology. Thus, the term antibody, as used herein,also includes antibody fragments either produced by the modification ofwhole antibodies, or those synthesized de novo using recombinant DNAmethodologies (e.g., single chain Fv) or those identified using phagedisplay libraries (see, e.g., McCafferty et al., Nature 348:552-554(1990)).

For preparation of monoclonal or polyclonal antibodies, any techniqueknown in the art can be used (see, e.g., Kohler & Milstein, Nature256:495-497 (1975); Kozbor et al., Immunology Today 4:72 (1983); Cole etal., pp. 77-96 in Monoclonal Antibodies and Cancer Therapy (1985)).“Monoclonal” antibodies refer to antibodies derived from a single clone.Techniques for the production of single chain antibodies (U.S. Pat. No.4,946,778) can be adapted to produce antibodies to polypeptides of thisinvention. Also, transgenic mice, or other organisms such as othermammals, may be used to express humanized antibodies. Alternatively,phage display technology can be used to identify antibodies andheteromeric Fab fragments that specifically bind to selected antigens(see, e.g., McCafferty et al., Nature 348:552-554 (1990); Marks et al.,Biotechnology 10:779-783 (1992)).

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a illustration showing DNA cleaving agents (appearing aseating faces) entering a permeabilized cell. For example, the cells canbe treated with a buffer that contains a permeabilization agent and aDNA cleaving agent. The cleaving agent enters the permeabilized cell anddigests genomic DNA (chromatin) that is in an open/accessibleconformation. Inaccessible chromatin is not digested.

FIG. 2 is a schematic representation of DNA inside the cell followingdigestion. The accessible chromatin is in small fragments and theinaccessible chromatin is, relatively, much larger.

FIG. 3 schematically represents a discovery provided herein, namely thatthe permeabilized cells allow small DNA fragments or protein-DNAcomplexes, corresponding to accessible chromatin, to diffuse out of thecell. The inaccessible chromatin is not digested and cannot diffuse outof the cell because it is too large to efficiently pass through thepermeabilized cell membrane.

FIG. 4 illustrates an embodiment of the invention in which permeabilizedand nuclease-treated cells are centrifuged. The cells, containinginaccessible chromatin, will be in the pellet and the supernatant willcontain accessible DNA that is relatively small in size.

FIG. 5 illustrates a BioAnalyzer tracing of the supernatant of Helacells that were permeabilized and treated with DNase I. A peak wasobserved in the 100-300 bp range, though some DNA was present over 2 kb.In contrast, DNA isolated from the cell would be much larger (over10,000 bp). This indicates that the DNA that diffused from thepermeabilized cells is indeed smaller than the bulk of DNA in the celland that the permeabilized cell is acting like a size filter for DNA.The sharp peaks at the low and high molecular weight ranges are sizestandards.

FIG. 6 illustrates qPCR analysis of the Hela sample (permeabilized andDNase I-treated). The GAPDH and RHO promoters were amplified. The GAPDHpromoter (left amplification curve), which is in accessible chromatin,is highly enriched relative to the RHO promoter (right amplificationcurve), which is in inaccessible chromatin. This indicates thataccessible chromatin is enriched in the supernatant from permeabilizedand DNase I-treated cells.

FIG. 7 provides next-generation sequencing data for DNA from thesupernatant of permeabilized and DNase I-treated Hela cells. The data ispresented to show regions within the genome where the supernatant DNAwas observed (“Inventive method” lane on the UCSC genome browser). Thedata was compared to publicly available data that maps accessiblechromatin regions on a genome-wide scale using other techniques (DigitalDNase and DNase-Seq lanes). The peaks for the supernatant DNA correlatewell with the peaks using the other techniques. This demonstrates thatmethod described herein maps accessible chromatin regions as well asother current, well characterized techniques. Notably, the methoddescribed herein is faster and requires less starting material than theother techniques, in addition, it does not require nuclei isolationwhich is a requirement of the other techniques.

FIG. 8 illustrates various types of molecules that can be targeted todiffuse from permeabilized cells treated with a DNA cleaving agent. Eachcolumn illustrates a possible target molecule in the supernatant(depending on how the assay is performed as described further herein),some possible ways to analyze the target molecule, comparative currentmethods for obtaining similar information, and finally some advantagesof the current method over the comparative method.

FIGS. 9A and 9B provide an exemplary BioAnalyzer tracing of mousetissue—kidney (9A) and brain (9B)—supernatant samples generatedaccording to the method described herein. This indicates that tissuesamples, as well as cells, can be used as starting material for themethods described herein.

FIG. 10 provides a qPCR analysis of the mouse tissue samples discussedin FIGS. 9A-B. In this qPCR analysis, the ACTB and TBP promoters, whichare known from other data to be in accessible chromatin, and the RHO andHBB promoters, which are in inaccessible chromatin, were amplified. TheACTB and TBP promoters were highly enriched relative to the RHO and HBBpromoters. This indicates that, as expected, accessible chromatin isenriched in the tissue samples and shows that the procedure is usefulfor tissue and biopsy samples.

FIG. 11 provides a summary of a method for detection of proteinsassociated with diffused DNA.

FIG. 12 shows that qPCR detects DNA bound to target proteins in activepromoter regions, but not inactive promoter regions.

FIG. 13 shows that the method depicted in FIG. 11 is more efficient thanstandard ChIP for detection of protein-associated active promoters

FIG. 14 shows that the method (left two columns) depicted in FIG. 11 hasa higher signal-to-noise ratio than standard ChIP (right two columns).

DETAILED DESCRIPTION OF THE INVENTION I. Introduction

The invention allows for analysis of chromatin structure by introducinga DNA cleaving agent into a permeabilized cell such that the DNAcleaving agent cleaves genomic DNA within the cell, and then separatingDNA fragments that diffuse out of the permeabilized cell from the cellitself. Without intending to limit the scope of the invention, it isbelieved that generally smaller fragments will diffuse out from thepermeabilized cell and that those smaller fragments represent genomicDNA regions in which the DNA cleaving agent had greater access comparedto other regions of genomic DNA. It is believed that accessibility ofthe DNA cleaving agent reflects the chromatin state of regions ofgenomic DNA. The smaller fragments, which generally diffuse out from thecell, represent regions that are more accessible to the DNA cleavingagent than larger fragments, which generally do not diffuse from thecell. By analyzing the smaller fragments that have diffused from thepermeabilized cell, or the larger fragments that do not diffuse, orboth, one can measure DNA cleaving accessibility, and thus indirectly,chromatin structure, for DNA regions of interest.

The varying accessibility of the DNA can reflect chromatin structure ofthe genomic DNA. For example, in some embodiments, DNA regions that aremore accessible to DNA cleaving agents are likely in more “loose”chromatin structures. Measurement of the chromatin state can provideuseful information regarding the biological state of a cell. Forexample, in some embodiments, the chromatin state of one of more DNAregions can provide diagnostic, prognostic, or other medicalinformation. As a non-limiting example, chromatin states can change as anormal cell progresses into cancer.

II. General Method

In one aspect, one or more DNA cleaving agent is introduced into a cellunder conditions such that genomic DNA is cleaved within the cell.Smaller cleaved fragments are then allowed to diffuse from thepermeabilized cell and the diffused DNA can then be separated from thepermeabilized cells, thereby allowing analysis of the diffused DNAand/or the DNA remaining in the permeabilized cell.

Permabilization of the cell can occur before, during, or after the DNAcleaving agent is introduced into the cell. An exogenous DNA cleavingagent will generally be introduced following or simultaneous withpermeabilization so that the DNA cleaving agent can enter the cell via“holes” in the cell generated by the permeabilizing step. In theseembodiments, the permeabilized cells can be incubated in a sufficientconcentration of the DNA cleaving agent to allow for the DNA cleavingagent to enter the cell. Alternatively, the DNA cleaving agent can beexpressed in (e.g., from an inducible promoter), or otherwise introducedinto (e.g., via electroporation), the cell prior to thepermeabilization. In these latter embodiments, permeabilization is notused to assist introduction of the DNA cleaving agents into the cell,but instead only provide exits by which the smaller cleaved DNAfragments can diffuse.

III. Permeabilizing Cells

Cell membranes can be permeabilized or disrupted in any way known in theart. The methods of permeabilizing or disrupting the cell membrane donot disrupt the structure of the genomic DNA of the cell such thatnucleosomal or chromatin structure is destroyed.

In some embodiments, the cell membrane is contacted with an agent thatpermeabilizes the cell membrane. Lysolipids are an exemplary class ofagents that permeabilize cell membranes. Exemplary lysolipids include,but are not limited to, lysophosphatidylcholine (also known in the artas lysolecithin) or monopalmitoylphosphatidylcholine. A variety oflysolipids are also described in, e.g., WO/2003/052095. The preciseconcentration of the agent will depend on the agent used as well, insome embodiments, to the cell to be permeabilized. As an example, insome embodiments, 0.25, 0.5%, 0.75 or 1% (or a concentration between0.25% and 1%) of lysolecithin (w/v) is used.

Non ionic detergents are an exemplary class of agents that disrupt cellmembranes. Exemplary nonionic detergents, include but are not limitedto, NP40, Tween 20 and Triton X-100. The precise concentration of theagent will depend on the non ionic detergent used as well, in someembodiments, to the cell to be permeabilized.

Alternatively, electroporation or biolistic methods can be used topermeabilize a cell membrane such that a DNA cleaving agent isintroduced into the cell and can thus contact the genomic DNA. A widevariety of electroporation methods are well known and can be adapted fordelivery of DNA modifying agents as described herein. Exemplaryelectroporation methods include, but are not limited to, those describedin WO/2000/062855. Biolistic methods include but are not limited tothose described in U.S. Pat. No. 5,179,022.

IV. DNA Cleaving Agents

Following, simultaneously with, or after permeabilization, a DNAcleaving agent is introduced into the cell such that the agent contactsand cleaves accessible genomic DNA in the cell. A DNA cleaving agent isany agent that introduces a double-stranded DNA break in DNA. A widevariety of DNA cleaving agents can be used according to the presentinvention. DNA cleaving agents can be, for example, a protein withdouble stranded DNA cleaving activity or a chemical having sufficientsteric hindrance such that differences in accessibility occur withingenomic DNA in the cell.

In some embodiments, the DNA cleaving agent(s) are contacted to thepermeabilized cells following removal of the permeabilizing agent,optionally with a change of the buffer. Alternatively, in someembodiments, the DNA cleaving agent is contacted to the genomic DNAwithout one or more intervening steps (e.g., without an exchange ofbuffers, washing of the cells, etc.). This latter approach can beconvenient for reducing the amount of labor and time necessary and alsoremoves a potential source of error and contamination in the assay.

The quantity of DNA cleaving agent used, as well as the time of thereaction, will depend on the agent used. Those of skill in the art willappreciate how to adjust conditions depending on the agent used.Generally, the conditions of the DNA cleaving step are adjusted suchthat a “complete” digestion is not achieved. Thus, for example, in someembodiments, the conditions of the cleaving step is set such that thepositive control—i.e., the control where cleavage sites areaccessible—occurs at a high level but less than 100%, e.g., between50-60%, 60-70%, 70-80%, 80-95%, 80-99%, 85-95%, 90-98%, etc.

In some embodiments, the DNA cleaving agent cleaves modified DNA, butnot unmodified DNA. In other embodiments, the DNA cleaving agent cleavesunmodified DNA but not modified DNA. In some of these embodiments, theDNA cleaving agent is used in combination with a DNA modifying agent(discussed further herein), thereby detecting accessible.

A. Restriction Enzymes

In some embodiments, the DNA cleaving agent is a restriction enzyme. Awide variety of restriction enzymes are known and can be used in thepresent invention.

Any type of restriction enzyme can be used. Type I enzymes cut DNA atrandom far from their recognition sequences. Type II enzymes cut DNA atdefined positions close to or within their recognition sequences. SomeType II enzymes cleave DNA within their recognition sequences. Type II-Senzymes cleave outside of their recognition sequence to one side. Thethird major kind of type II enzyme, more properly referred to as “typeIV,” cleave outside of their recognition sequences. For example, thosethat recognize continuous sequences (e.g., AcuI: CTGAAG) cleave on justone side; those that recognize discontinuous sequences (e.g., BcgI:CGANNNNNNTGC) cleave on both sides releasing a small fragment containingthe recognition sequence. Type III cleave outside of their recognitionsequences and require two such sequences in opposite orientations withinthe same DNA molecule to accomplish cleavage.

The methods of the invention can be adapted for use with any type ofrestriction enzyme or other DNA cleaving enzyme. In some embodiments,the enzyme cleaves relatively close (e.g., within 5, 10, or 20 basepairs) of the recognition sequence. Such enzymes can be of particularuse in assaying chromatin structure as the span of DNA that must beaccessible to achieve cutting is larger than the recognition sequenceitself and thus may involve a wider span of DNA that is not in a “tight”chromatin structure.

In some embodiments, more than one (e.g., two, three, four, etc.)restriction enzymes are used. Combinations of enzymes can involvecombinations of enzymes all from one type or can be mixes of differenttypes.

In some embodiments, the restriction enzyme is a modification-sensingrestriction enzyme, meaning that the restriction enzyme is eithermodification-dependent (i.e., cleaving in the presence but not absenceof modifications in the recognition sequence) or methylation-sensitive(i.e., cleaving in the absence but not presence of modifications in therecognition sequence). An exemplary modification is, e.g., DNAmethylation or DNA acetylation.

DNA methylation can occur in several different types, including at theN⁶ position of adenosine and at the C⁴ and C⁵ positions of cytosine(which can be methylation of hydroxymethylation). A number ofmethyl-adenosine sensing and methyl-cytosine sensing restriction enzymesare known. Exemplary N⁶-methyl-adenosine sensitive restriction enzymesinclude, e.g., DpnII. Exemplary N⁶-methyl-adenosine dependentrestriction enzymes include, e.g., DpnII. Exemplary methyl-cytosinesensitive restriction enzymes include, e.g., MspI and GlaI. Exemplarymethyl-cytosine dependent restriction enzymes include, e.g., MspJI.

In some embodiments, the restriction enzyme is a hydroxymethyl cytosinesensing restriction enzyme. For example, PvuRTS 1 is a hydroxymethylcytosine-dependent restriction enzyme (Janosi et al., J. Mol. Biol.242:45-61 (1994)) and can be used as the DNA cleaving agent, therebyidentifying accessible or inaccessible regions having or lackinghydroxymethyl cytosine.

B. DNases

In some embodiments, an enzyme that cleaves DNA in a sequencenon-specific manner is used as a DNA cleaving agent. Thus, in someembodiments, the DNA cleaving agent is a sequence non-specificendonuclease (also referred to herein as a “DNase”).

Any sequence non-specific endonuclease (e.g., micrococcal nuclease(MNase) or any of DNase I, II, III, IV, V, VI, VII) can be usedaccording to the present invention. For example, any DNase, includingbut not limited to, DNase I and MNase can be used. MNases can inducedouble stand breaks within nucleosome linker regions, but onlysingle-strand breaks within the nucleosome itself. DNases used caninclude naturally occurring DNases as well as modified DNases. Anexample of a modified DNase is TURBO DNase (Ambion), which includesmutations that allow for “hyperactivity” and salt tolerance. ExemplaryDNases, include but are not limited, to Bovine Pancreatic DNase I(available from, e.g., New England Biolabs).

C. Fusion Proteins

In some embodiments, the DNA cleaving or modifying agents are fused orotherwise linked to a heterologous double-stranded sequence-non-specificnucleic acid binding domain (e.g., a DNA binding domain), a heterologoussequence-specific nucleic acid binding (i.e., a “DNA-recognition”)polypeptide, or a heterologous protein binding (i.e., a“protein-recognition”) polypeptide. In cases where the DNA cleaving ormodifying agent is a polypeptide, the DNA cleaving or modifying agentand the heterologous polypeptide can be generated as a singlepolypeptide, synthesized, for example, as a protein fusion viarecombinant DNA technology.

A double-stranded sequence-non-specific nucleic acid binding domain is aprotein or defined region of a protein that binds to double-strandednucleic acid in a sequence-independent manner, i.e., binding does notexhibit a gross preference for a particular sequence. A double-strandedsequence-non-specific nucleic acid binding domain fusion can haveimproved activity compared to the DNA cleaving or modifying agentlacking the double-stranded sequence-non-specific nucleic acid bindingdomain. In some embodiments, double-stranded nucleic acid bindingproteins exhibit a 10-fold or higher affinity for double-stranded versussingle-stranded nucleic acids. The double-stranded nucleic acid bindingproteins in some embodiments of the invention are thermostable. Examplesof such proteins include, but are not limited to, the Archaeal smallbasic DNA binding proteins Sac7d and Sso7d (see, e.g., Choli et al.,Biochimica et Biophysica Acta 950:193-203, 1988; Baumann et al.,Structural Biol. 1:808-819, 1994; and Gao et al, Nature Struc. Biol.5:782-786, 1998), Archael HMf-like proteins (see, e.g., Starich et al.,J. Molec. Biol. 255:187-203, 1996; Sandman et al., Gene 150:207-208,1994), and PCNA homologs (see, e.g., Cann et al., J. Bacteriology181:6591-6599, 1999; Shamoo and Steitz, Cell: 99, 155-166, 1999; DeFelice et al., J. Molec. Biol. 291, 47-57, 1999; and Zhang et al.,Biochemistry 34:10703-10712, 1995). See also European Patent 1283875B1for addition information regarding DNA binding domains.

Sso7d and Sac7d are small (about 7,000 kd MW), basic chromosomalproteins from the hyperthermophilic archaeabacteria Sulfolobussolfataricus and S. acidocaldarius, respectively. These proteins arelysine-rich and have high thermal, acid and chemical stability. Theybind DNA in a sequence-independent manner and when bound, increase theT_(M) of DNA by up to 40° C. under some conditions (McAfee et al.,Biochemistry 34:10063-10077, 1995). These proteins and their homologsare typically believed to be involved in stabilizing genomic DNA atelevated temperatures.

The HMf-like proteins are archaeal histones that share homology both inamino acid sequences and in structure with eukaryotic H4 histones, whichare thought to interact directly with DNA. The HMf family of proteinsform stable dimers in solution, and several HMf homologs have beenidentified from thermostable species (e.g., Methanothermus fervidus andPyrococcus strain GB-3a). The HMf family of proteins, once joined to TaqDNA polymerase or any DNA modifying enzyme with a low intrinsicprocessivity, can enhance the ability of the enzyme to slide along theDNA substrate and thus increase its processivity. For example, thedimeric HMf-like protein can be covalently linked to the N terminus ofTaq DNA polymerase, e.g., via chemical modification, and thus improvethe processivity of the polymerase.

Those of skill in the art will recognize that other double-strandedsequence-non-specific nucleic acid binding domain are known in the artand can also be used as described herein.

The heterologous sequence-specific nucleic acid binding (i.e., a“DNA-recognition”) polypeptide allows for targeting of the DNA cleavingor modifying agent to particular DNA sequences in the cell, therebyallowing one to assay the accessibility of specific DNA sequences in thegenome. A wide variety of sequence specific DNA binding polypeptides anddomains are known and can be used as fusion partners with the DNAcleaving or modifying agent as desired. Exemplary sequence-specific DNAbinding polypeptides include, but are not limited to, zinc fingerdomains, TAL domains, etc.

The heterologous protein-recognition polypeptide (i.e. a polypeptidethat specifically binds a particular protein or class of proteins)allows for targeting of the DNA cleaving or modifying agent toparticular protein associated with genomic DNA, thereby targetinggenomic DNA that is both accessible to the agent and in proximity to theparticular targeted protein. A wide variety of protein-recognitionpolypeptides and domains are known and can be used as fusion partnerswith the DNA cleaving or modifying agent as desired. Exemplaryprotein-recognition polypeptides include, but are not limited to,antibodies.

V. DNA Modifying Agents

In addition to the DNA cleaving agents, one or more DNA modifying agentscan also be introduced into the permeabilized cells. DNA modifyingagents generate a covalent modification to the DNA. In some cases, theDNA modifying agent is introduced before or simultaneously with the DNAcleaving agent. In some embodiments, the DNA modifying agent isintroduced to the cell simultaneously with the permeabilizing agent andsubsequently, the DNA cleaving agent is introduced into the cell. Insome embodiments, the DNA cleaving agent is a modification-sensingenzyme, wherein the DNA cleaving agent only cleaves modified DNA or DNAcontaining a modified recognition sequence, or alternatively, onlycleaves unmodified DNA or DNA containing an unmodified recognitionsequence.

For example, in some embodiments, the DNA modifying agents of theinvention are methyltransferases. A variety of methyltransferases areknown in the art and can be used in the invention. In some embodiments,the methyltransferase used adds a methyl moiety to adenosine in DNA.Examples of such methyltransferases include, but are not limited to, DAMmethyltransferase. Because adenosine is not methylated in eukaryoticcells, the presence of a methylated adenosine in a particular DNA regionfollowing treatment of the cell with an adenosine methyltransferase(e.g., a DAM methyltransferase or other methyltransferase with similaractivity) indicates that it was able to access the DNA region. Adenosinemethylation can be detected, for example, using as a DNA cleaving agenta restriction enzyme whose recognition sequence includes a methylatedadenosine. An example of such an enzyme includes, but is not limited to,DpnI. Cutting by the restriction enzyme can be detected and quantifiedby measuring the identity and amount of DNA fragments that diffuse fromthe cells.

In some embodiments, the methyltransferase methylates cytosines in GCsequences. Examples of such methyltransferases include but are notlimited to MCviPI. See, e.g., Xu et al., Nuc. Acids Res. 26(17):3961-3966 (1998). Because GC sequences are not methylated in eukaryoticcells, the presence of a methylated GC sequence in a particular DNAregion indicates that the DNA modifying agent (i.e., a methyltransferasethat methylates cytosines in GC sequences) was able to access the DNAregion. Methylated GC sequences can be identified using any number oftechniques. In some embodiments, the method for detecting methylated GCsequences comprises bisulfite conversion. Bisulfite conversion involvescontacting the DNA with a sufficient amount of bisulfite to convertunmethylated cytosines to uracil. Methylated cytosines are notconverted. Thus, DNA regions containing a GC sequence can be contactedwith a methyltransferase that methylates cytosines in GC sequences,isolated, and then contacted with bisulfite. If the C in the GC sequenceis not methylated, the C will be converted to U (or T if subsequentlyamplified), whereas a methylated C will remain a C. Any number ofmethods, including but not limited to, nucleotide sequencing and methodsinvolving primer extension or primer-based amplification and/ormethylation-sensitive restriction digests can be used to detect thepresence or absence of a bisulfite converted C (e.g., MSnuPE, MSP orMethyllight, high resolution melt analysis; pyrosequencing, etc.). See,e.g., Fraga, et al., Biotechniques 33:632, 634, and 636-649 (2002);El-Maarri O Adv Exp Med Biol 544:197-204 (2003); Laird, Nat Rev Cancer3:253-266 (2003); and Callinan, Hum Mol Genet. 15 Spec No 1:R95-101(2006).

In some embodiments, the methyltransferase methylates cytosines in CG(also known as “CpG”) sequences. Examples of such methyltransferasesinclude but are not limited to M.SssI. Use of such methyltransferaseswill generally be limited to use for those DNA regions that are nottypically methylated. This is because CG sequences are endogenouslymethylated in eukaryotic cells and thus it is not generally possible toassume that a CG sequence is methylated by the modifying agent ratherthan an endogenous methyltransferase except in such DNA regions wheremethylation is rare. As for GC sequences, methylation of CG sequencescan be detected by any number of methods, including methods involvingbisulfite conversion.

In some embodiments, the DNA modifying agent comprises a DNA modifyingchemical. As most DNA modifying chemicals are relatively small comparedto chromatin, use of DNA modifying chemicals without a fusion partnermay not be effective in circumstances in which the chemical isintroduced into the cell because there will be little if any differencein the extent of accessibility of different DNA regions. Therefore, insome embodiments, the DNA modifying agent comprises a molecule havingsteric hindrance linked to a DNA modifying chemical. The molecule havingsteric hindrance can be any protein or other molecule that results indifferential accessibility of the DNA modifying agent depending onchromatin structure. This can be tested, for example, by comparingresults to those using a DNase or restriction enzyme as describedherein.

In some embodiments, the molecule having steric hindrance will be atleast 5, 7, 10, or 15 kD in size. Those of skill in the art will likelyfind it convenient to use a polypeptide as the molecule with sterichindrance. Any polypeptide can be used that does not significantlyinterfere with the DNA modifying agent's ability to modify DNA. In someembodiments, the polypeptide is a double-stranded sequence-non-specificnucleic acid binding domain as discussed in further detail herein.

The DNA modifying chemicals of the present invention can be linkeddirectly to the molecule having steric hindrance or via a linker. Avariety of homo and hetero bifunctional linkers are known and can beused for this purpose.

VI. Separating Diffused DNA from Permeabilized Cells

Following DNA cleavage in the cell and cell permeabilization, thesmaller DNA fragments and/or protein/DNA complexes are allowed todiffuse from the cell. After an appropriate amount of time has elapsedfor diffusion to occur, the diffused DNA and/or protein/DNA complexesare subsequently separated from the cell. Separation can readily beachieved, for example, by centrifuging the cells following diffusion,thereby pelleting the intact permeabilized cells. See, e.g., FIG. 4. Insome embodiments, separation will comprise one or more filtrations usingfilters that block cell passage but allow DNA passage.

The diffused DNA can be any size, but as noted herein, is expected to besmaller than DNA retained in the permeabilized cell. As DNA retained inthe cell will generally be 10,000 base pairs or larger, in someembodiments, the diffused DNA is generally less than 10,000 bp, e.g.,less than 5,000 bp, less than 3,000 bp, less than 1,000 bp, e.g.,between 5-1,000 bp, 50-500, 50-1000 bp, 50-5,000 bp, or 50-10,000 bp.

The supernatant containing the diffused DNA can be removed, andoptionally the diffused DNA can be further purified.

In some embodiments, the DNA remaining in the permeabilized cells ispurified from the cells following separation from the diffused DNA. Anytype of DNA purification from the cells can be used as desired. The DNAremaining in the cell represents DNA that was relatively inaccessible tothe DNA cleaving agent and thus can be analyzed to determine theidentity of DNA regions that are inaccessible. In some embodiments,diffused and non-diffused DNA are both analyzed and optionally compared,for example as a control to each other.

In some embodiments, the non-diffused genomic DNA in the permeabilizedcell is purified according to any method available. Essentially any DNApurification procedure can be used so long as it results in DNA ofacceptable purity for the subsequent analysis step(s). For example,standard cell lysis reagents can be used to lyse cells. Optionally aprotease (including but not limited to proteinase K) can be used. DNAcan be isolated from the mixture as is known in the art. In someembodiments, phenol/chloroform extractions are used and the DNA can besubsequently precipitated (e.g., by ethanol) and purified. In someembodiments, RNA is removed or degraded (e.g., with an RNase or with useof a DNA purification column), if desired. Optionally, genomic DNA isamplified or otherwise detected directly from the cell lysate without anintermediate purification step.

VII. Analyzing DNA and/or Protein

DNA and proteins that diffuse from the permeabilized cell can beanalyzed in any way useful to the user. Thus, the following is notintended to be an exhaustive listing. Analysis can include, but need notbe limited to, determining the identity and/or quantity of a particularmolecule (e.g., a DNA sequence or protein). Analysis can also include,for example, cloning the DNA, sequencing the DNA or analyzing the DNAusing microarrays.

It is believed that both DNA and chromatin protein or other DNA bindingproteins in association with the DNA can diffuse from the cellsfollowing cleavage and permeabilization. Similarly, it is believed thatin some embodiments, RNA in association with the DNA can diffuse fromthe cells following cleavage and permeabilization. In some embodiments,the diffused DNA is analyzed. In some embodiments, the associatedprotein is analyzed. In some embodiments, both the diffused DNA andassociated proteins are analyzed. In some embodiments, the RNA isanalyzed. In some embodiments, the DNA and RNA are analyzed. Moreover,as explained herein, in some embodiments, the DNA that did not diffusefrom the cell can be purified from the cell and analyzed. This DNA willin some embodiments provide a control or “mirror image” result from thediffused DNA. Thus, unless indicated otherwise, to the extent thefollowing discussion refers to “DNA,” it refers equally to diffused DNAor DNA that did not diffuse and was isolated from the permeabilizedcells after the diffused DNA was separated from the cell(s).

In some embodiments, prior to DNA analysis, the DNA (i.e., enriched fromDNA fragments leaked, and optionally separated, from the permeabilizedcell) is enriched for one or more particular DNA sequences, for example,by affinity purifying particular DNA sequences using a nucleic acidprobe (optionally linked to a solid support (e.g., a bead)) underappropriate hybridization conditions. In other embodiments the DNA isaffinity-purified using an antibody or non-antibody protein (such as,but not limited to, a transcription factor, a transcription factorprotein or DNA-binding fragment thereof, or a methyl-DNA bindingprotein) that binds to DNA.

Alternatively, in situations in which there are proteins in associationwith the diffused DNA, DNA in association with the proteins can befurther purified from other DNA by selectively binding the protein withan affinity agent that specifically binds the protein and then purifyingthe protein and associated DNA from other DNA not in association withthe protein. See, FIG. 8. It will be appreciated that any agent havingaffinity (e.g., that specifically binds) with the protein can be used inthis way. In some embodiments, the agent is an antibody specific for aparticular protein. In other embodiments the affinity agent is anon-antibody protein. The protein associated with the DNA can be anyDNA-binding protein, including but not limited to, chromatin proteins,histones (including but not limited to H3K4me histone H3. i.e., histoneH3 trimethylated at lysine 4), transcription factors, RNA polymerase,and TATA box binding protein (TBP). In some embodiments, the protein andassociated DNA are immunoprecipitated, thereby separating the DNAassociated with the protein from other DNA. In other embodiments, theaffinity agent (e.g., antibody), linked directly or indirectly to asolid support, is incubated with the supernatant of a permeabilized cellunder conditions to bind the affinity agent to the target bindingprotein complexed with DNA fragments. The resulting complex (affinityagent, target protein, fragmented DNA) can then be separated from thesupernatant, thereby purifying the target DNA binding protein andassociated DNA. Any solid support can be used. In some embodiments, thesolid support is a bead or particle. In some embodiments, the bead orparticle is magnetic, or can be attracted to a magnet, thereby allowingfor efficient purification from the supernatant when desired. Ifdesired, the presence, absence or quantity of DNA associated with aprotein can be analyzed (e.g., amplified, sequenced, detected, etc.) andoptionally compared between samples, including but not limited, betweendiseased and healthy samples.

In some embodiments, DNA associated with proteins is analyzed bynucleotide sequencing. See, FIG. 8. For example, sequencing processesthat can simultaneous detect nucleotide sequence and distinguish whethersequenced nucleotides are modified can be used. Examples of the lattertype of sequencing include, but are not limited to, single-moleculereal-time (SMRT) sequencing and nanopore sequencing. Results from suchanalyses is similar to that obtained from ChIP-Seq (see, e.g., Johnsonet al., Science 316: 1497-1502 (2007)), but provides data only foraccessible sequences, which may be advantageous in some instances asaccessible chromatin is thought to be the functionally active regions ofthe genome.

In some embodiments, multiple (e.g., two or more) DNA fragments diffusefrom the cell in a complex with one or more protein. See, FIG. 8, rightcolumn. In some embodiments, the DNA and/or proteins in the complex areanalyzed. In some embodiments, these complexes are purified from theremaining DNA and then analyzed. In some embodiments, the complexes arecontacted with a DNA ligase, thereby ligating the multiple DNA fragmentstogether, which can subsequently be analyzed by any way desired (e.g.,amplified, hybridized, sequenced, etc.). This analysis will provide, forexample, information regarding associations and interactions ofaccessible chromatin regions.

DNA Analysis

In some embodiments, following isolation of DNA of interest, the DNA iscloned into a library. In some cases, one or more specific DNA sequenceis isolated and/or cloned. Alternatively, the DNA is used to prepare alibrary (either representing diffused DNA or non-diffused DNA).

In some embodiments, subtractive libraries are generated. For example,libraries can be generated that are enriched for a diseased celldiffused or non-diffused DNA regions in the methods of the invention andsubsequently subtracted with a corresponding library from a healthycell, or vice versa, thereby generating a library of differential DNAsequences specific for the particular disease. Any diseased cell can beused, including but not limited to, cancer cells. Alternate subtractivestrategies can also be employed, e.g., between different cell types,cell stages, drug treatments, etc.

Analysis can include determination of any physical characteristic of theDNA. Physical characteristics include, but are not limited to, DNAmethylation, melting temperature, GC content, nucleotide sequence, andability to hybridize to a polynucleotide or ability to be amplified. Avariety of methods are known for detecting such characteristics and canbe employed.

In some embodiments, the physical characteristic is DNA methylation. Forexample, once relatively accessible DNA has been cleaved by a DNAcleaving agent, one can isolate the remaining intact DNA (representingless accessible DNA) and can then be analyzed for methylation status. Alarge variety of DNA methylation detection methods are known. In someembodiments, the DNA is contacted with bisulfite, thereby convertingunmethylated cytosines to uracils in the DNA. The methylation of aparticular DNA region can then be determined by any number ofmethylation detection methods, including those discussed herein. In someembodiments, a high resolution melt assay (HRM) is employed to detectmethylation status following bisulfite conversion. In this method, a DNAregion is amplified following bisulfite conversion and the resultingamplicon's melting temperature is determined. Because the meltingtemperature will differ depending on whether the cytosines wereconverted by bisulfite (and subsequently copied as “T's” in theamplification reaction), melting temperature of the amplicon can becorrelated to methylation content.

In some embodiments, one or more DNA sequence is amplified, for exampleusing end point or quantitative amplification techniques (e.g., qPCR).In some embodiments, one or more specific primers are used tospecifically amplify a particular sequence with in the DNA. Quantitativeamplification (including, but not limited to, real-time PCR) methodsallow for determination of the amount of intact copies of a DNA region,and can be used with various controls to determine the relative amountof copies of the DNA region in a sample of interest (e.g., as diffusedfrom a permeabilized cell or not diffused from the cell), therebyindicating whether and to what extent a specific DNA region(s) isaccessible.

Quantitative amplification methods (e.g., quantitative PCR orquantitative linear amplification) involve amplification of nucleic acidtemplate, directly or indirectly (e.g., determining a Ct value)determining the amount of amplified DNA, and then calculating the amountof initial template based on the number of cycles of the amplification.Amplification of a DNA locus using reactions is well known (see U.S.Pat. Nos. 4,683,195 and 4,683,202; PCR PROTOCOLS: A GUIDE TO METHODS ANDAPPLICATIONS (Innis et al., eds, 1990)). Typically, PCR is used toamplify DNA templates. However, alternative methods of amplificationhave been described and can also be employed, as long as the alternativemethods amplify intact DNA to a greater extent than the methods amplifycleaved or degraded DNA. Methods of quantitative amplification aredisclosed in, e.g., U.S. Pat. Nos. 6,180,349; 6,033,854; and 5,972,602,as well as in, e.g., Gibson et al., Genome Research 6:995-1001 (1996);DeGraves, et al., Biotechniques 34(1):106-10, 112-5 (2003); Deiman B, etal., Mol. Biotechnol. 20(2):163-79 (2002). Amplifications can bemonitored in “real time.”

In some embodiments, quantitative amplification is based on themonitoring of the signal (e.g., fluorescence of a probe) representingcopies of the template in cycles of an amplification (e.g., PCR)reaction. In the initial cycles of the PCR, a very low signal isobserved because the quantity of the amplicon formed does not support ameasurable signal output from the assay. After the initial cycles, asthe amount of formed amplicon increases, the signal intensity increasesto a measurable level and reaches a plateau in later cycles when the PCRenters into a non-logarithmic phase. Through a plot of the signalintensity versus the cycle number, the specific cycle at which ameasurable signal is obtained from the PCR reaction can be deduced andused to back-calculate the quantity of the target before the start ofthe PCR. The number of the specific cycles that is determined by thismethod is typically referred to as the cycle threshold (Ct). Exemplarymethods are described in, e.g., Heid et al. Genome Methods 6:986-94(1996) with reference to hydrolysis probes.

In some embodiments, the nucleotide sequence of one or more DNAfragment, or a sequence thereof, is determined. For example, a genomicDNA sequence for a sample of interest can be sequenced and compared tocorresponding known genomic DNA sequences in order to determine sites ofDNA accessibility or inaccessibility in the sample of interest. Methodsof nucleic acid sequencing are well-known in the art. Examples ofsequence analysis include, but are not limited to, Maxam-Gilbertsequencing, Sanger sequencing, capillary array DNA sequencing, thermalcycle sequencing (Sears et al., Biotechniques, 13:626-633 (1992)),solid-phase sequencing (Zimmerman et al., Methods Mol. Cell. Biol.,3:39-42 (1992)), sequencing with mass spectrometry such asmatrix-assisted laser desorption/ionization time-of-flight massspectrometry (MALDI-TOF/MS; Fu et al., Nature Biotech., 16:381-384(1998)), and sequencing by hybridization (Chee et al., Science,274:610-614 (1996); Drmanac et al., Science, 260:1649-1652 (1993);Drmanac et al., Nature Biotech., 16:54-58 (1998)).

A variety of methods can be used to determine the nucleotide sequenceand, if desired, the extent to which sequenced nucleotides are modified,e.g., methylated, either naturally within the cell or by an introducedDNA modifying agent. Any sequencing method known in the art can be used.In some embodiments, the sequencing method simultaneously determines thenucleotide sequence and whether sequenced nucleotides are modified. Forexample, as the sequencing process determines the order of nucleotidesin a nucleic acid fragment, at the same time it can also distinguishbetween modified nucleotides (e.g., methylated nucleotides) andnon-modified nucleotides (e.g., non-methylated nucleotides). Examples ofsequencing processes that can simultaneous detect nucleotide sequenceand distinguish whether sequenced nucleotides are modified include, butare not limited to, single-molecule real-time (SMRT) sequencing andnanopore sequencing.

In some embodiments, nucleotide sequencing comprises template-dependentreplication of the DNA region that results in incorporation of labelednucleotides (e.g., fluorescently labeled nucleotides), and wherein anarrival time and/or duration of an interval between signal generatedfrom different incorporated nucleotides is determinative of the presenceor absence of the modification and/or the identity of an incorporatednucleotide.

Single-Molecule, Real-Time Sequencing

In some embodiments, genomic DNA comprising a target DNA region issequenced by single-molecule, real-time (SMRT) sequencing. SMRTsequencing is a process by which single DNA polymerase molecules areobserved in real time while they catalyze the incorporation offluorescently labeled nucleotides complementary to a template nucleicacid strand. Methods of SMRT sequencing are known in the art and wereinitially described by Flusberg et al., Nature Methods, 7:461-465(2010), which is incorporated herein by reference for all purposes.

Briefly, in SMRT sequencing, incorporation of a nucleotide is detectedas a pulse of fluorescence whose color identifies that nucleotide. Thepulse ends when the fluorophore, which is linked to the nucleotide'sterminal phosphate, is cleaved by the polymerase before the polymerasetranslocates to the next base in the DNA template. Fluorescence pulsesare characterized by emission spectra as well as by the duration of thepulse (“pulse width”) and the interval between successive pulses(“interpulse duration” or “IPD”). Pulse width is a function of allkinetic steps after nucleotide binding and up to fluorophore release,and IPD is a function of the kinetics of nucleotide binding andpolymerase translocation. Thus, DNA polymerase kinetics can be monitoredby measuring the fluorescence pulses in SMRT sequencing.

In addition to measuring differences in fluorescence pulsecharacteristics for each fluorescently-labeled nucleotide (i.e.,adenine, guanine, thymine, and cytosine), differences can also bemeasured for non-methylated versus methylated bases. For example, thepresence of a methylated base alters the IPD of the methylated base ascompared to its non-methylated counterpart (e.g., methylated adenosineas compared to non-methylated adenosine). Additionally, the presence ofa methylated base alters the pulse width of the methylated base ascompared to its non-methylated counterpart (e.g., methylated cytosine ascompared to non-methylated cytosine) and furthermore, differentmodifications have different pulse widths (e.g., 5-hydroxymethylcytosinehas a more pronounced excursion than 5-methylcytosine). Thus, each typeof non-modified base and modified base has a unique signature based onits combination of IPD and pulse width in a given context. Thesensitivity of SMRT sequencing can be further enhanced by optimizingsolution conditions, polymerase mutations and algorithmic approachesthat take advantage of the nucleotides' kinetic signatures, anddeconvolution techniques to help resolve neighboring methylcytosinebases.

Nanopore Sequencing

In some embodiments, nucleotide sequencing does not comprisetemplate-dependent replication of a DNA region. In some embodiments,genomic DNA comprising a target DNA region is sequenced by nanoporesequencing. Nanopore sequencing is a process by which a polynucleotideor nucleic acid fragment is passed through a pore (such as a proteinpore) under an applied potential while recording modulations of theionic current passing through the pore. Methods of nanopore sequencingare known in the art; see, e.g., Clarke et al., Nature Nanotechnology4:265-270 (2009), which is incorporated herein by reference for allpurposes.

Briefly, in nanopore sequencing, as a single-stranded DNA moleculepasses through a protein pore, each base is registered, in sequence, bya characteristic decrease in current amplitude which results from theextent to which each base blocks the pore. An individual nucleobase canbe identified on a static strand, and by sufficiently slowing the rateof speed of the DNA translocation (e.g., through the use of enzymes) orimproving the rate of DNA capture by the pore (e.g., by mutating keyresidues within the protein pore), an individual nucleobase can also beidentified while moving.

In some embodiments, nanopore sequencing comprises the use of anexonuclease to liberate individual nucleotides from a strand of DNA,wherein the bases are identified in order of release, and the use of anadaptor molecule that is covalently attached to the pore in order topermit continuous base detection as the DNA molecule moves through thepore. As the nucleotide passes through the pore, it is characterized bya signature residual current and a signature dwell time within theadapter, making it possible to discriminate between non-methylatednucleotides. Additionally, different dwell times are seen betweenmethylated nucleotides and the corresponding non-methylated nucleotides(e.g., 5-methyl-dCMP has a longer dwell time than dCMP), thus making itpossible to simultaneously determine nucleotide sequence and whethersequenced nucleotides are modified. The sensitivity of nanoporesequencing can be further enhanced by optimizing salt concentrations,adjusting the applied potential, pH, and temperature, or mutating theexonuclease to vary its rate of processivity.

In some embodiments, the DNA is hybridized to another nucleic acid. Insome embodiments, the nucleic acid is linked to a solid support. Forexample, in some embodiments, the DNA is hybridized to a microarray. Amicroarray is useful, for example, in monitoring the presence, absenceor quantity of multiple sequences in the DNA. In some embodiments, DNAfrom different samples can be hybridized to one or more nucleic acids,thereby determining the differential amount of one or more particularsequence between the samples, Thus, for example, diseased and healthycells, or cells obtained at different times, or before and after orduring treatment can be compared.

The present methods can include correlating accessibility of a DNAregion to transcription from that same region. In some embodiments,experiments are performed to determine a correlation betweenaccessibility and gene expression and subsequently accessibility of aDNA modifying agent to a particular DNA region can be used to predicttranscription from the DNA region. In some embodiments, transcriptionfrom a DNA region and accessibility of that region to DNA modifyingagents are both determined. A wide variety of methods for measuringtranscription are known and include but are not limited to, the use ofnorthern blots and RT-PCR.

In some embodiments, the DNA methylation status of a region can becorrelated with accessibility of a DNA region to the DNA modifyingagent. In some embodiments, experiments are performed to determine acorrelation between accessibility and DNA methylation in the region andsubsequently accessibility of a DNA modifying agent to a particular DNAregion can be used to predict DNA methylation from the DNA region. Insome embodiments, methylation of a DNA region and accessibility of thatregion to DNA modifying agents are both determined. A wide variety ofmethods for measuring DNA methylation are known and include but are notlimited to, the use of bisulfite (e.g., in sequencing and/or incombination with methylation-sensitive restriction enzymes (see, e.g.,Eads et al., Nucleic Acids Research 28(8): E32 (2002)) and the highresolution melt assay (HRM) (see, e.g., Wodjacz et al, Nucleic AcidsResearch 35(6):e41 (2007)).

In some embodiments, comparisons of the presence, absence, or quantityof a first DNA region in the diffused smaller DNA fragments and/or inthe non-diffused larger DNA is compared with the presence, absence, orquantity of a second DNA region from the same cell(s). In someembodiments, the second DNA region is a control region, e.g., a DNAregion that is known to be accessible or inaccessible. Alternatively, orin addition, one can compare presence, absence, or quantity of a firstDNA region in the diffused smaller DNA fragments and/or in thenon-diffused larger DNA in two different cells. For example, the twocells can represent diseased and healthy cells or tissues, differentcell types, different stages of development (including but not limitedto stem cells or progenitor cells), cells obtained at different timesfrom an individual, etc. Thus, by using the methods of the invention onecan detect differences in chromatin structure between cells and/ordetermine relative chromatin structures between two or more DNA regions(e.g., genes) within one cell. In addition, one can determine the effectof a drug, chemical or environmental stimulus on the chromatin structureof a particular region in the same cells or in different cells.

Protein Analysis

As noted above, in addition to DNA analysis, protein associated with thediffused DNA can also be analyzed. The protein can be analyzed asdesired. In some embodiments, the protein(s) is microsequenced todetermine its amino acid sequence. In some embodiments, the protein isanalyzed with one or more immunuological method. For example, anantibody of known specificity can be contacted to the protein todetermine whether the protein binds the antibody, thereby suggesting theprotein's identity.

VIII. Samples

A variety of eukaryotic cells can be used in the present invention. Insome embodiments, the cells are animal cells, including but not limitedto, human, or non-human, mammalian cells. Non-human mammalian cellsinclude but are not limited to, primate cells, mouse cells, rat cells,porcine cells, and bovine cells. In some embodiments, the cells arenon-mammalian cells, e.g., avian, reptilian, or other cells. In someembodiments, the cells are plant cells. Cells can be, for example,cultured primary cells, immortalized culture cells or can be from abiopsy or tissue sample, optionally cultured and stimulated to dividebefore assayed. Cultured cells can be in suspension or adherent prior toand/or during the permeabilization and/or DNA modification steps. Insome embodiments, the cells can be from a tumor biopsy.

IX. Diagnostic and Prognostic Methods

The present invention also provides methods for diagnosing or providinga prognosis for a disease or condition or determining a course oftreatment for a disease or condition based on the accessibility orinaccessibility of DNA regions in genomic DNA.

In some embodiments, accessibility of a DNA region of interest to a DNAcleaving agent is increased (or at least is present) or decreased (orabsent) in a diseased cell or tissue as compared to a normal (i.e.,non-diseased) cell or tissue. In these embodiments, detection of thepresence or absence or quantity of copies of the DNA region of interestcan be used as a diagnostic or prognostic tool.

Once a diagnosis or prognosis is established using the methods of theinvention, a regimen of treatment can be established or an existingregimen of treatment can be altered in view of the diagnosis orprognosis. For instance, detection of a cancer cell according to themethods of the invention can lead to the administration ofchemotherapeutic agents and/or radiation to an individual from whom thecancer cell was detected.

A variety of DNA regions can be detected either for research purposesand/or as a control DNA region to confirm that the reagents wereperforming as expected. For example, in some embodiments, a DNA regionis assayed that is known to be accessible or inaccessible. Such DNAregions are useful, for example, as positive or negative controls foraccessibility.

X. Kits

The present invention also provides kits for performing the methodsdescribed herein. A kit can optionally include written instructions orelectronic instructions (e.g., on a CD-ROM or DVD). Kits of the presentinvention can include, e.g., a DNA modifying agent and/or a DNA cleavingagent; a cell permeabilization agent; and an affinity agent thatspecifically binds to a DNA-binding protein. The DNA cleaving agent cancomprise, for example, a DNase or a restriction enzyme or a DNA cleavingpolypeptide fused to a heterologous DNA-recognition polypeptide. The DNAmodifying agent can be, for example, a DNA methyltransferase. Thepermeabilization agent can be, for example, a lysolipid or a nonionicdetergent. The affinity agent can, for example, specifically bind to ahistone, a modified histone, an RNA polymerase, a transcription factor,a TATA box-binding protein (TBP), or other DNA-binding protein and canbe, e.g., an antibody. In some cases, the affinity agent is linked to asolid support. Exemplary solid supports include, e.g., a bead orparticle. In some embodiments, the bead or particle is magnetic orattracted to magnets.

The kits of the invention can also include one or more control cellsand/or nucleic acids. Exemplary control nucleic acids include, e.g.,those comprising a gene sequence that is either accessible inessentially all cells of an animal (e.g., a housekeeping gene sequenceor promoter thereof) or inaccessible in most cells of an animal. In someembodiments, the kits include one or more sets of primers for amplifyingsuch gene sequences (whether or not the actually gene sequences or cellsare included in the kits). For example, in some embodiments, the kitsinclude a DNA modifying agent, a DNA cleaving agent, and a cellpermeabilizing and/or cell disrupting agent, an affinity agent thatspecifically binds to a DNA-binding protein, and one or more primer setsfor amplifying a control DNA region (including but not limited to acontrol gene as described herein), and optionally one or more primersets for amplifying a second DNA region, e.g., a target DNA region.

EXAMPLES Example 1

This example demonstrates that small DNA fragments can be obtained frompermeabilized Hela cells following introduction of DNase I into thecells. Hela cells were grown in a standard 6-well tissue culture plateto 95% confluence, about 1 million cells per well. The culture media wasaspirated and 500 μl of a permeabilization/digestion buffer was gentlylayered on the cells. The permeabilization/digestion buffer consisted oflysolecithin, Tris-HCl, MgCl₂, CaCl₂ and DNase I. The permeabilizedcells were then incubated at 37° C. for 30 minutes. Following incubationthe permeabilization/digestion buffer was collected in a 1.5 mleppendorf tube and placed on ice for 2 minutes. The sample was thencentrifuged in a microcentrifuge at 13,000 rpm for 2 minutes and thesupernatent was transferred to a new 1.5 ml eppendorf tube. The samplewas then re-centrifuged at 13,000 rpm for 5 min and 400 μl of thesupernatent was transferred to a new 1.5 ml eppendorf tube. 100 ul oflysis/stop buffer was then added to the sample; the sample was mixed andincubated at 37° C. for 10 minutes. The lysis/stop buffer consisted ofTris-HCl, NaCl, EDTA, N-lauroylsarcosine, RNase A and proteinase K. TheDNA was then isolated using a commercial nucleic acid purification kit(Aurum, Bio-Rad) following standard procedures. 1 ul of each sample wasthen analyzed using the high sensitivity chip in the BioAnalyzer(Agilent). 10 ul each sample was diluted to 50 ul and analyzed by qPCRon a Bio-Rad CFX 384-well real time PCR instrument using RHO and GAPDHprimer sets and the following protocol: 96° C. for 5 minutes followed by40 cycles of 96° C. for 30 seconds/66° C. for 1 minute.

FIG. 5 illustrates a BioAnalyzer tracing of the supernatant of Helacells that were permeabilized and treated with DNase I. A peak wasobserved in the 100-300 bp range, though some DNA was present over 2 kb.In contrast, DNA isolated from the cell would be much larger (over10,000 bp). This indicates that the DNA in the supernatant is indeedsmaller than the bulk of DNA in the cell and that the permeabilized cellis acting like a size filter for DNA.

DNA in the supernatant was also analyzed by qPCR. Specifically, GAPDHand RHO promoters were amplified using the following protocol: 96° C.for 5 minutes followed by 40 cycles of 96° C. for 30 seconds/66° C. for1 minute. As illustrated in FIG. 6, the GAPDH promoter (leftamplification curve), which is in accessible chromatin, was highlyenriched relative to the RHO promoter (right amplification curve), whichis in inaccessible chromatin. This indicated that accessible chromatinis enriched in the supernatant from permeabilized and DNaseI-treatedcells.

DNA in the supernatant of the permeabilized and DNase I-treated Helacells was also sequenced on an Illumina Genome Analyzer II using a 36cycle single-end sequencing protocol. FIG. 7 provides a summary ofsequencing results of DNA from the supernatant. FIG. 7 shows regionswithin the genome where the supernatant DNA was observed (“Inventivemethod” lane on the UCSC genome browser). The data was compared topublicly available data that maps accessible chromatin regions on agenome-wide scale using other techniques (Digital DNase and DNase-Seqlanes). The peaks for the supernatant DNA correlate well with the peaksusing the other techniques. This demonstrates that method describedherein maps accessible chromatin regions as well as the other current,well characterized techniques. Notably, the method described herein isfaster, requires less starting material, and does not require nucleiisolation.

Example 2

This example demonstrates that small DNA fragments can be obtained frompermeabilized cells from tissue samples following introduction of DNaseI into the cells.

FIGS. 9A and 9B provide an exemplary BioAnalyzer tracing of mousetissue—kidney (9A) and brain (9B)—supernatant samples generatedaccording to the method described herein. This indicates that tissuesamples, as well as cells, can be used as starting material.

Similar to Example 1, supernatant DNA from the tissue was submitted toquantitative PCR. In this case, two promoters known to be accessible(the ACTB and TBP promoters), and two promoters known to be inaccessible(the RHO and HBB promoters), were amplified. See, FIG. 10. The ACTB andTBP promoters were highly enriched relative to the RHO and HBBpromoters. This indicates that, as expected, accessible chromatin isenriched in the tissue samples and shows that the procedure will work intissue and biopsy samples.

Example 3

This example demonstrates that DNA binding proteins associated withgenomic DNA can be obtained from permeabilized cells. The example alsodemonstrates that DNA complexed with DNA-binding proteins can beenriched (and subsequently analyzed) using an agent that specificallybinds the target DNA-binding protein.

Chromatin immunoprecipitation (ChIP) is a powerful tool that identifiesDNA regions associated with specific proteins, transcription factors, orhistone variants. It can be used to map transcription regulation andcontrol elements genome-wide. As explained above, a novel technology forisolating active chromatin was been developed. When permeabilized cellsare treated with a nuclease, small DNA fragments, corresponding toactive chromatin, diffuses out of cell and can be collected. These smallDNA fragments, when analyzed, for example, by next-generationsequencing, provide a global map of active chromatin regions.

We show in this example that the active chromatin that has diffused fromthe cell is still associated with its cognate DNA-binding proteins andhistones. Based on this finding, a novel ChIP method that does notrequire protein-DNA cross-linking or DNA shearing is provided. Usingthis method (1) RNA polymerase II (RNAPII), (2) TBP and (3) histone H3trimethylated on lysine 4 (H3K4me3) were each demonstrated to beassociated with active promoters, but rarely detected at silencedpromoters. Comparison of the ChIP method described herein with astandard ChIP assay shows that immunoprecipitation (IP) efficiency issimilar, but IP specificity is dramatically different. To measure IPspecificity, the ratio of active promoter DNA precipitated with RNAPII(signal) was compared relative to inactive promoter DNA precipitated(noise). We find that the new ChIP method described here yields highlyspecific IP with a signal-to-noise ratio of >300; however standard ChIPis much less specific with a signal-to-noise ratio of about 6. Weconclude that the new ChIP method described here offers two significantadvantages over standard ChIP: dramatically reduced background and amuch easier workflow.

As depicted in FIG. 3, DNA fragments from active chromatin diffuse outof cells after nuclease treatment. Proteins that bind to their targetDNA sites will also diffuse out of the cell and into the supernatant.When physiological cell conditions are provided, these proteins willmaintain binding status to their DNA target sites. To verify thatproteins are still bound to their target sites from diffused DNAfragments we choose RNAPII, TATA box binding protein (TBP) and H3K4 m3,three proteins known to bind to active promoters but not inactivepromoters.

Our general approach is depicted in FIG. 11. Briefly, Hela cells weregrown and treated with DNase I as described above and subsequentlycentrifuged and the supernatant was removed. The supernatant wasincubated with antibodies specific for RNAII, TBP or H3K4 m3 linked tomagnetic beads via protein G, centrifuged, and the supernatant wasremoved. The beads were washed and subsequently eluted by incubating thebeads with 500 μl of 1 mM TRIS-HCl, pH 8.5 and incubated at 95° C. for 5minutes. qPCR analyses were performed using primers that amplifypromoter regions from active or silenced genes to detect DNA in theeluate.

The results (see FIG. 12) show that qPCR detected protein bound to DNAin the active (GAPDH) promoter region for all three proteins, butdetected little protein bound to DNA in the inactive (RHO) promoterregion.

We also compared our data with standard ChIP technology and showed thatthe inventive assay depicted in FIG. 11 has similar or better detectionefficiency than standard ChIP technology. See, FIG. 13.

Further, we used qPCR-detected RNAPII bound DNA from active promoterGAPDH as signal and from inactive promoter RHO as noise to determine ourmethod's and standard ChIP's specificity. The results (FIG. 14) show ourmethod has a dramatic signal-to-noise ratio than standard ChIP.

To generate additional data we performed next-generation sequencing ofthe samples that were analyzed by qPCR. The sequencing was performed onan Illumina Genome Analyzer IIx using a 36 base, single-end readprotocol. The reads were mapped to the human genome (hg19) and a bigWigfile indicating tag-count was generated. The data from the bigWig fileswas mapped back to the human genome and visualized on the UCSC genomebrowser. We found that our method was better at detecting biologicallyrelevant protein-DNA interactions than traditional ChIP analysesperformed by the ENCODE consortium and publically available on the UCSCGenome Browser (data not shown).

We developed a novel method for identifying protein binding sites in thegenome. This new ChIP assay does not require DNA-protein cross linkingand DNA shearing. It makes running a ChIP assay much easier. Our methoddetects proteins bound to active DNA regions in the genome. Itdramatically reduces assay background. Comparing with standard ChIPassay our assay is more specific for its targets, having a dramatichigher signal-to-noise ratio than standard ChIP. This will provide, forexample, more accurate genome-wide mapping of gene regulation network.

It is understood that the examples and embodiments described herein arefor illustrative purposes only and that various modifications or changesin light thereof will be suggested to persons skilled in the art and areto be included within the spirit and purview of this application andscope of the appended claims. All publications, patents, and patentapplications cited herein are hereby incorporated by reference in theirentirety for all purposes.

1. A method of separating DNA accessible to a DNA cleaving agent in apermeabilized cell from DNA inaccessible to the DNA cleaving agent, themethod comprising: permeabilizing a cell having genomic DNA, therebygenerating a permeabilized cell; introducing a DNA cleaving agent intothe permeabilized cell having genomic DNA under conditions such that theDNA cleaving agent cleaves the genomic DNA in the cell, therebygenerating cleaved DNA; and separating cleaved DNA that diffuses out ofthe intact permeabilized cell from the cell.
 2. The method of claim 1,further comprising introducing a DNA modifying agent into thepermeabilized cell such that the DNA modifying agent modifies thegenomic DNA in the cell.
 3. The method of claim 2, wherein the DNAmodifying agent and the DNA cleaving agent are introduced simultaneouslyor the DNA modifying agent is introduced before the DNA cleaving agentis introduced.
 4. The method of claims 2, wherein the DNA cleaving agentis DNase I or micrococcal nuclease.
 5. The method of claim 3, whereinthe DNA modifying agent adds modifications to at least some recognitionsequences of the DNA cleaving agent, and the DNA cleaving agent does notcleave recognition sequences with the modification.
 6. The method ofclaim 3, wherein the DNA modifying agent adds modifications to at leastsome recognition sequences of the DNA cleaving agent, and the DNAcleaving agent cleaves recognition sequences with the modification anddoes not cleave recognition sequences lacking the modification.
 7. Themethod of claim 2, wherein the DNA modifying agent is a DNAmethyltransferase.
 8. The method of claim 2, wherein the DNA modifyingagent is introduced after the DNA cleaving agent is introduced.
 9. Themethod of claim 1, wherein the permeabilizing and the introducing occursimultaneously.
 10. The method of claim 1, further comprising isolatingthe cleaved DNA.
 11. The method of claim 1, further comprising isolatingDNA remaining in the intact cell following the separating.
 12. Themethod of claim 1, wherein the DNA cleaving agent comprises a DNAcleaving polypeptide fused to a heterologous DNA-recognitionpolypeptide.
 13. The method of claim 1, wherein the isolating comprisesaffinity purifying the DNA.
 14. The method of claim 1, furthercomprising analyzing the separated DNA.
 15. The method of claim 14,wherein the analyzing comprises nucleotide sequencing the separated DNA.16. The method of claim 14, wherein the analyzing comprises anamplification reaction.
 17. The method of claim 14, wherein two or morenucleic acids are associated with one or more proteins and the analyzingcomprises ligating the two or more nucleic acids.
 18. The method ofclaim 10, wherein the isolated DNA is associated with one or moreprotein.
 19. The method of claim 1, wherein the separating comprisescentrifuging and/or filtering the permeabilized cell thereby separatinga solution containing the cleaved DNA from the cell.
 20. A kitcomprising a DNA modifying agent and/or a DNA cleaving agent; a cellpermeabilization agent; and an affinity agent that specifically binds toa DNA-binding protein.